A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958264



Internal ID39493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157918466..157921223hg38UCSC Ensembl
chr4:158839618..158842375hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg382758
hg192758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465623
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958264
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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